NDC 42549-549

NDC 42549-549

NDC 42549-549 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 42549-549
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 42549-549-60 [42549054960]

tizanidine hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076280
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-11-26
Inactivation Date2019-11-13

NDC 42549-549-90 [42549054990]

tizanidine hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076280
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-11-26
Inactivation Date2019-11-13

NDC 42549-549-04 [42549054904]

tizanidine hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076280
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-11-26
Inactivation Date2019-11-13

NDC 42549-549-30 [42549054930]

tizanidine hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076280
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-11-26
Inactivation Date2019-11-13

NDC 42549-549-12 [42549054912]

tizanidine hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076280
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-11-26
Inactivation Date2019-11-13

NDC 42549-549-28 [42549054928]

tizanidine hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076280
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-11-26
Inactivation Date2019-11-13

Drug Details

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.